Functional <i>FOXC1</i> variants in familial and sporadic atrial septal defect with cellular and animal validation-Reference-Cited by-同舟云学术

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Functional FOXC1 variants in familial and sporadic atrial septal defect with cellular and animal validation

Published:2024-06-25 Issue:7 Volume:14 Page:
ISSN:2001-1326
Container-title:Clinical and Translational Medicine
language:en
Short-container-title:Clinical & Translational Med

Author:

Chen Huan‐Xin¹²,Hou Hai‐Tao¹²,Wang Xiu‐Li¹²,Wang Jun¹²,Yang Qin¹²,He Guo‐Wei¹²^ORCID

Affiliation:

1. Department of Cardiac Surgery and The Institute of Cardiovascular Diseases TEDA International Cardiovascular Hospital, Tianjin University and Chinese Academy of Medical Science Tianjin China

2. Tianjin Key Laboratory of Molecular Regulation of Cardiovascular Diseases and Translational Medicine Tianjin China

Funder

National Natural Science Foundation of China

Tianjin Municipal Science and Technology Bureau

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ctm2.1676

Reference10 articles.

1. Genetics and Genomics of Congenital Heart Disease

2. Involvement of a novel GATA4 mutation in atrial septal defects

3. The murine winged helix transcription factors, Foxc1 and Foxc2, are both required for cardiovascular development and somitogenesis

4. Essential structural and functional determinants within the forkhead domain of FOXC1

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